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Synfacts 2018; 14(03): 0259
DOI: 10.1055/s-0037-1609264
DOI: 10.1055/s-0037-1609264
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
Enantioselective Cycloaddition of Cyclopropylcarboxamides to Alkynes
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
15. Februar 2018 (online)
Key words
nickel catalysis - aluminum catalysis - cycloaddition - cyclopropylcarbox-amides - alkynesSignificance
Transition-metal-catalyzed cycloaddition of cyclopropanes to π-unsaturated compounds is a useful method for the formation of cyclic compounds that has been studied over recent decades. However, the reaction with cyclopropylcarboxamides remains challenging due to their relatively low reactivity. The authors have developed a Ni–Al bimetallic system that facilitates the cycloaddition reaction of cyclopropylcarboxamides to alkynes.
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Comment
Whereas a nonenantioselective reaction was achieved by using Ph2P(O)H as a bifunctional ligand, a TADDOL-derived chiral ligand realized highly enantioselective cycloaddition reactions.
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